Department of Pharmacology, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, 980-8575, Japan.
Division of Pharmacology, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, 4-4-1 Komatsushima, Aoba-ku, Sendai, 981-8558, Japan.
Sci Rep. 2017 Nov 21;7(1):15899. doi: 10.1038/s41598-017-16019-8.
Histamine is a neurotransmitter that regulates diverse physiological functions including the sleep-wake cycle. Recent studies have reported that histaminergic dysfunction in the brain is associated with neuropsychiatric disorders. Histamine N-methyltransferase (HNMT) is an enzyme expressed in the central nervous system that specifically metabolises histamine; yet, the exact physiological roles of HNMT are unknown. Accordingly, we phenotyped Hnmt knockout mice (KO) to determine the relevance of HNMT to various brain functions. First, we showed that HNMT deficiency enhanced brain histamine concentrations, confirming a role for HNMT in histamine inactivation. Next, we performed comprehensive behavioural testing and determined that KO mice exhibited high aggressive behaviours in the resident-intruder and aggressive biting behaviour tests. High aggression in KO mice was suppressed by treatment with zolantidine, a histamine H2 receptor (H2R) antagonist, indicating that abnormal H2R activation promoted aggression in KO mice. A sleep analysis revealed that KO mice exhibited prolonged bouts of awakening during the light (inactive) period and compensatory sleep during the dark (active) period. Abnormal sleep behaviour was suppressed by treatment with pyrilamine, a H1R antagonist, prior to light period, suggesting that excessive H1R activation led to the dysregulation of sleep-wake cycles in KO mice. These observations inform the physiological roles of HNMT.
组胺是一种神经递质,调节包括睡眠-觉醒周期在内的多种生理功能。最近的研究报告称,大脑中的组胺能功能障碍与神经精神疾病有关。组氨酸 N-甲基转移酶(HNMT)是一种在中枢神经系统中表达的酶,专门代谢组胺;然而,HNMT 的确切生理作用尚不清楚。因此,我们对 Hnmt 敲除小鼠(KO)进行表型分析,以确定 HNMT 与各种大脑功能的相关性。首先,我们表明 HNMT 缺乏会增强大脑组胺浓度,证实了 HNMT 在组胺失活中的作用。接下来,我们进行了全面的行为测试,确定 KO 小鼠在居民入侵者和攻击性行为测试中表现出高攻击性。KO 小鼠的高攻击性被组胺 H2 受体(H2R)拮抗剂唑拉啶抑制,表明异常的 H2R 激活促进了 KO 小鼠的攻击性。睡眠分析表明,KO 小鼠在光照(不活动)期表现出长时间的觉醒发作,并在黑暗(活动)期进行补偿性睡眠。在光照期前用 H1R 拮抗剂吡拉明治疗可抑制异常的睡眠-觉醒周期,表明过度的 H1R 激活导致 KO 小鼠睡眠-觉醒周期失调。这些观察结果说明了 HNMT 的生理作用。